List of variants reported as likely benign for Usher syndrome type 2A by Illumina Laboratory Services, Illumina

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg)	rs696723	0.06184
NM_206933.4(USH2A):c.2109T>C (p.Asp703=)	rs45555435	0.01476
NM_206933.4(USH2A):c.2522C>A (p.Ser841Tyr)	rs111033282	0.00569
NM_206933.4(USH2A):c.2546G>A (p.Cys849Tyr)	rs111033481	0.00424
NM_206933.4(USH2A):c.478G>A (p.Gly160Ser)	rs111033479	0.00240
NM_206933.4(USH2A):c.3395G>A (p.Gly1132Asp)	rs34596189	0.00216
NM_206933.4(USH2A):c.2256T>C (p.His752=)	rs111033281	0.00103
NM_206933.4(USH2A):c.1608C>T (p.Cys536=)	rs187380128	0.00014
NM_206933.4(USH2A):c.1935A>T (p.Thr645=)	rs146670690	0.00011
NM_206933.4(USH2A):c.3532C>G (p.Pro1178Ala)	rs372081834	0.00003

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